Details
| Type | Protein Coding |
| Official Symbol | CHCHD10 |
| Official Name | coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559] |
| Ensembl ID | ENSG00000273607 |
| Bio databases IDs | |
| Aliases | coiled-coil-helix-coiled-coil-helix domain containing 10 |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
- Myopathy isolated mitochondrial autosomal dominant
- Spinal muscular atrophy jokela type